Extracellular Ca2+ and its effect on acid extrusion in the crayfish stretch receptor neurone

1996 ◽  
Vol 199 (8) ◽  
pp. 1781-1789
Author(s):  
H Moser ◽  
N Mair ◽  
F Fresser

1. In the stretch receptor neurones of the crayfish Astacus astacus, the intracellular pH (pHi), the intracellular Na+ concentration ([Na+]i) and the membrane potential (Em) were measured simultaneously using ion-selective and conventional microelectrodes. Normal Astacus saline (NAS), and salines containing varying amounts of Ca2+ (Ca2+-NAS) but of constant ionic strength, with Na+, Mg2+ or Ba2+ as substituting ions, were used to investigate the effects of extracellular Ca2+ concentration ([Ca2+]o) on pHi and pHi regulation, on [Na+]i and on Em. The maximum rate of pHi recovery was used as a measure of pHi regulation. Acid loads were imposed using the NH4+/NH3 rebound technique. 2. [Ca2+]o affected pHi, pHi regulation, [Na+]i and Em. The magnitudes of the effects were inversely related to [Ca2+]o and were specific to the ion used for [Ca2+]o substitution. 3. Compared with controls, increasing [Ca2+]o threefold (in exchange for Na+) elicited some alkalization, a 7 % faster maximum rate of pHi recovery and generally lower values of [Na+]i. 4. In low-Ca2+ or Ca2+-free NAS (substitutions by Na+ or Mg2+), pHi became more acid, the maximum rate of pHi recovery was reduced by up to 50 % and [Na+]i was generally higher. The effects were faster and larger at lower [Ca2+]o, and stronger with Na+ than with Mg2+ as the substituting ion. 5. In Ca2+-free NAS (Ca2+ substituted for by Ba2+), the effects on pHi, on the maximum rate of pHi recovery and on [Na+]i were generally small. In this respect, Ba2+ had similar physiological properties to Ca2+ and was almost equally effective. 6. Changes in Em, including rapid depolarizations and occasional burst activity in Ca2+-free NAS, indicate that alterations in the properties of the membrane, such as a change in its permeability or selectivity, are occurring. Measurements of [Na+]i support this view. In addition, Ba2+ per se induced a (small) depolarization, as shown when Ba2+ was present in NAS or in low-Ca2+ NAS. 7. Changes in [Ca2+]o affected [Na+]i. *[Na+]i is defined as [Na+]i determined at the onset of the maximum rate of pHi recovery, and the ratio *[Na+]i/[Na+]o at that instant was calculated. A linear relationship between the maximum rate of pHi recovery and the *[Na+]i/[Na+]o ratio was found, irrespective of the amount and of the ion species used for [Ca2+]o substitution. This is strong evidence that pHi and pHi regulation were indirectly affected by [Ca2+]o, which altered membrane properties and thus caused a change in [Na+]i. We could find no evidence for a direct contribution of [Ca2+]o to acid extrusion or to a direct modulatory action on the transport protein of the Na+/H+ antiporter.

1993 ◽  
Vol 178 (1) ◽  
pp. 109-124
Author(s):  
N. Mair ◽  
H. Moser ◽  
F. Fresser

Regulation of intracellular pH (pHi) following acidosis induced by NH4+/NH3 exposures was re-investigated in a crayfish stretch receptor neurone using H+- and Na+-selective microelectrodes. All experiments were performed in nominally HCO3-/CO2-free salines. From studies in Na+-free saline and from electrochemical calculations, we concluded that pHi regulation was dependent on extracellular Na+ concentration ([Na+]o). The half-maximal rate of pHi recovery had an apparent Michaelis-Menten constant of 21 mmol l-1 [Na+]o. The use of this experimental approach and an improved technique enabled us to observe pHi regulation even in Cl-- free saline, in contrast to earlier findings. In addition, amiloride (2 mmol l-1) inhibited the maximum rate of pHi recovery by about 80 %, SITS (1 mmol l- 1) by about 20 %. The results strongly suggest the operation of two separate pHi-regulating mechanisms, a Na+-dependent HCO3-/Cl- antiporter (probably the Na+/H+/HCO3-/Cl- antiporter described earlier) and a Na+/H+ antiporter. Both mechanisms have been described in crayfish ganglion cells and muscle fibres, but the individual contribution to pHi regulation varies considerably in these preparations. Functional aspects of the pHi-regulating mechanisms in relation to ionic changes during the moulting cycle are discussed.


2019 ◽  
pp. 76-98
Author(s):  
Gordon L. Fain

“Mechanoreceptors and touch” is the fifth chapter of the book Sensory Transduction and describes general mechanisms of touch sensitivity in animals. It begins with a review of mechanoreception in the single-celled protozoan Paramecium and transduction of touch in the round worm Caenorhabditis elegans. A thorough treatment is next given of the crayfish stretch receptor and insect mechanoreceptors, including a description of NOMPC channels in Drosophila. The chapter then reviews the anatomy and physiology of mechanoreceptors and touch in mammals, both in glabrous and hairy skin. It concludes with recent discoveries of the molecular biology and physiology of Merkel cells, known to be responsible for much of mammalian touch sensation.


1999 ◽  
Vol 82 (4) ◽  
pp. 1843-1854 ◽  
Author(s):  
Marzia Martina ◽  
Sébastien Royer ◽  
Denis Paré

Mounting evidence implicates the central (CE) nucleus of the amygdala in the mediation of classically conditioned fear responses. However, little data are available regarding the intrinsic membrane properties of CE amygdala neurons. Here, we characterized the physiological properties of CE medial (CEM) and CE lateral (CEL) amygdala neurons using whole cell recordings in brain slices maintained in vitro. Several classes of CE neurons were distinguished on the basis of their physiological properties. Most CEM cells (95%), here termed “late-firing neurons,” displayed a marked voltage- and time-dependent outward rectification in the depolarizing direction. This phenomenon was associated with a conspicuous delay between the onset of depolarizing current pulses and the first action potential. During this delay, the membrane potential ( V m) depolarized slowly, the steepness of this depolarizing ramp increasing as the prepulse V m was hyperpolarized from −60 to −90 mV. Low extracellular concentrations of 4-aminopyridine (30 μM) reversibly abolished the outward rectification and the delay to firing. Late-firing CEM neurons displayed a continuum of repetitive firing properties with cells generating single spikes at one pole and high-frequency (≥90 Hz) spike bursts at the other. In contrast, only 56% of CEL cells displayed the late-firing behavior prevalent among CEM neurons. Moreover, these CEL neurons only generated single spikes in response to membrane depolarization. A second major class of CEL cells (38%) lacked the characteristic delay to firing observed in CEM cells, generated single spikes in response to membrane depolarization, and displayed various degrees of inward rectification in the hyperpolarizing direction. In both regions of the CE nucleus, two additional cell types were encountered infrequently (≤ 6% of our samples). One type of neurons, termed “low-threshold bursting cells” had a behavior reminiscent of thalamocortical neurons. The second type of cells, called “fast-spiking cells,” generated brief action potentials at high rates with little spike frequency adaptation in response to depolarizing current pulses. These findings indicate that the CE nucleus contains several types of neurons endowed with distinct physiological properties. Moreover, these various cell types are not distributed uniformly in the medial and lateral sector of the CE nucleus. This heterogeneity parallels anatomic data indicating that these subnuclei are part of different circuits.


1968 ◽  
Vol 51 (5) ◽  
pp. 635-654 ◽  
Author(s):  
Shosaku Obara ◽  
Harry Grundfest

Unlike several other varieties of input membrane, that of the crayfish stretch receptor develops a generator potential in response to stretch when all the Na of the medium is replaced with Li. However, Li depolarizes the receptor neuron, the soma membrane becoming more depolarized than that of the axon. During exposure to Li the cell usually fires spontaneously for a period, and when it becomes quiescent spike electrogenesis fails in the soma but persists in the axon. These effects are seen in the rapidly adapting as well as the slowly adapting cells. The block of spike electrogenesis of the soma membrane is only partly due to the Li-induced depolarization and a significant role must be ascribed to a specific effect of Li.


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